# FDA recall Z-1194-2018

> **Arrow International Inc** · Class II · device recall initiated 2017-12-15.

## Product

ARROW ENDURANCE" Extended Dwell Peripheral Catheter System, Catalog Numbers: EDC-00820 & EDC-00820-B

## Reason for recall

Certain lots of peripheral catheter systems may be missing the safety latch, intended to minimize the risk of sharps injuries.

## Distribution

Distributed in the following U.S. states: CO, FL, IL, NC, PA, SC, and TX.

## Key facts

- **Recall number:** Z-1194-2018
- **Recalling firm:** Arrow International Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-12-15
- **Report date:** 2018-04-04
- **Termination date:** 2019-07-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Reading, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1194-2018

## Citation

> AI Analytics. FDA recall Z-1194-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-1194-2018. Source: US FDA. Licensed CC0.

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